A Co-Promoted Ni-B Amorphous Nanoalloy Catalyst for Liquid Phase Hydrogenation of Furfural to Furfural Alcohol

2011 ◽  
Vol 183-185 ◽  
pp. 2322-2326 ◽  
Author(s):  
Chang Hai Du ◽  
Yong Zhao ◽  
De Sun
Keyword(s):  
Aqueous Solution ◽  
Liquid Phase ◽  
Room Temperature ◽  
Chemical Reduction ◽  
Amorphous Structure ◽  
Cobalt Acetate ◽  
Nickel Acetate ◽  
Liquid Phase Hydrogenation

The Co-promoted Ni-B amorphous nanoalloy catalysts were prepared by the chemical reduction of the aqueous solution containing nickel acetate and cobalt acetate with NaBH4 at room temperature and characterized by BET, XRD and DSC. They were used as catalysts for the liquid phase hydrogenation of furfural to furfural alcohol in alcohol at 353 K under 2.0 MPa of hydrogen. Ni-Co-B catalyst was characterized by XRD as amorphous structure. It was active in the hydrogenation of furfural, and it was significantly more active than Ni-B and Co-B. The optimal Co/ ( Co+Ni ) mole ratio in Ni-Co-B was 0.5.

scholarly journals Solvent-free hydrogenation of cyclohexene over Rh-TUD-1 at ambient conditions

RSC Advances ◽  
2018 ◽  
Vol 8 (60) ◽  
pp. 34370-34373 ◽  
Author(s):  
Mhamed Benaissa ◽  
Abdullah M. Alhanash ◽  
Ahmed T. Mubarak ◽  
Morad Eissa ◽  
Taher Sahlabji ◽  
...  
Keyword(s):  
Liquid Phase ◽  
Room Temperature ◽  
Hydrogenation Reaction ◽  
Solvent Free ◽  
Ambient Conditions ◽  
Total Conversion ◽  
Free System ◽  
Liquid Phase Hydrogenation ◽  
System P ◽  
Solvent Free System

Total conversion of cyclohexene to cyclohexane was achieved in a liquid phase hydrogenation reaction at room temperature, 1 atm H2 pressure and solvent-free system.

scholarly journals Synthesis of cobalt nanowires in aqueous solution under an external magnetic field

2016 ◽  
Vol 7 ◽  
pp. 990-994 ◽  
Author(s):  
Xiaoyu Li ◽  
Lijuan Sun ◽  
Hu Wang ◽  
Kenan Xie ◽  
Qin Long ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Aqueous Solution ◽  
External Magnetic Field ◽  
Room Temperature ◽  
Magnetic Measurements ◽  
Chemical Reduction ◽  
Average Diameter ◽  
Firm Structure ◽  
Cobalt Nanowires ◽  
First Time

In contrast to the majority of related experiments, which are carried out in organic solvents at high temperatures and pressures, cobalt nanowires were synthesized by chemical reduction in aqueous solution with the assistance of polyvinylpyrrolidone (PVP) as surfactant under moderate conditions for the first time, while an external magnetic field of 40 mT was applied. Uniform linear cobalt nanowires with relatively smooth surfaces and firm structure were obtained and possessed an average diameter of about 100 nm with a coating layer of PVP. By comparison, the external magnetic field and PVP were proven to have a crucial influence on the morphology and the size of the synthesized cobalt nanowires. The prepared cobalt nanowires are crystalline and mainly consist of cobalt as well as a small amount of platinum. Magnetic measurements showed that the resultant cobalt nanowires were ferromagnetic at room temperature. The saturation magnetization (M s) and the coercivity (H c) were 112.00 emu/g and 352.87 Oe, respectively.

The superior performance of a Pt catalyst supported on nanoporous SiC–C composites for liquid-phase selective hydrogenation of cinnamaldehyde

RSC Advances ◽  
2016 ◽  
Vol 6 (84) ◽  
pp. 81211-81218 ◽  
Author(s):  
Ruihua Yao ◽  
Junrui Li ◽  
Peng Wu ◽  
Xiaohong Li
Keyword(s):  
Liquid Phase ◽  
Selective Hydrogenation ◽  
Room Temperature ◽  
Superior Performance ◽  
Pt Catalyst ◽  
Unsaturated Alcohol ◽  
Liquid Phase Hydrogenation

The Pt/SiC–C catalyst: active, selective (80% selectivity to unsaturated alcohol) and reusable for liquid-phase hydrogenation of cinnamaldehyde at room temperature.

Study on deactivation of Ni/Al2O3 catalyst for liquid phase hydrogenation of crude 1,4-butanediol aqueous solution

2012 ◽  
Vol 181-182 ◽  
pp. 501-507 ◽  
Author(s):  
Haitao Li ◽  
Yongxiang Zhao ◽  
Chunguang Gao ◽  
Yongzhao Wang ◽  
Zijin Sun ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Liquid Phase ◽  
Liquid Phase Hydrogenation ◽  
Al2o3 Catalyst

scholarly journals Influence of Synthesis Parameters of FeNi3 Alloy Nanoparticles Obtained by Chemical Reduction Method in Aqueous Solution

2019 ◽  
Vol 70 (4) ◽  
pp. 1118-1124
Author(s):  
Teodora Malaeru ◽  
Eros Alexandru Patroi ◽  
Delia Patroi ◽  
Eugen Manta ◽  
Virgil Marinescu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Chemical Reduction ◽  
Molar Ratio ◽  
Initial Reaction ◽  
Growth Promoter ◽  
Stoichiometric Ratio ◽  
Alloy Nanoparticles ◽  
Face Centered Cubic ◽  
Structural Morphology

This paper reports the synthesis of FeNi3 alloy nanoparticles by chemical reduction of the Fe2+ and Ni2+ ions, from the corresponding chlorides, with hydrazine (N2H4�H2O) as a reducing agent in aqueous solution at room temperature by modifying the molar ratio of the ions Fe2+: Ni2+, reaction time, with and without amine-type growth promoter, and reducing both, with or without ultrasonic aid. The FeNi3 alloy nanoparticles have been investigated by XRD, EDS spectrum analysis, SEM and VSM. When the molar ratio of Fe2+ and Ni2+ is equal to 1:3, reducing both, with or without ultrasonic aid, Fe2+ and Ni2+ were completely reduced into Fe and Ni, resulting FeNi3 alloy with a face-centered cubic (fcc) crystal structure. EDS analysis supported the presence of metal ions in atomic weight corresponding to the stoichiometric ratio of initial reaction. SEM analysis showed that nanoparticles of FeNi3 alloy have a spherical structural morphology. Hysteresis loop show a ferromagnetic behaviour of the FeNi3 alloy nanoparticles at room temperature.

Spherulite Structures in a Melt Spun Fe-Ni Austenitic Steel

1985 ◽  
Vol 43 ◽  
pp. 52-53
Author(s):  
G. M. Michal ◽  
T. K. Glasgow ◽  
T. J. Moore
Keyword(s):  
Austenitic Steel ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Large Range ◽  
Amorphous Structure ◽  
Nucleation And Growth ◽  
Ni Alloys ◽  
Melt Spun ◽  
Crystal Fibers ◽  
Rapidly Solidified

Large additions of B to Fe-Ni alloys can lead to the formation of an amorphous structure, if the alloy is rapidly cooled from the liquid state to room temperature. Isothermal aging of such structures at elevated temperatures causes crystallization to occur. Commonly such crystallization pro ceeds by the nucleation and growth of spherulites which are spherical crystalline bodies of radiating crystal fibers. Spherulite features were found in the present study in a rapidly solidified alloy that was fully crysstalline as-cast. This alloy was part of a program to develop an austenitic steel for elevated temperature applications by strengthening it with TiB2. The alloy contained a relatively large percentage of B, not to induce an amorphous structure, but only as a consequence of trying to obtain a large volume fracture of TiB2 in the completely processed alloy. The observation of spherulitic features in this alloy is described herein. Utilization of the large range of useful magnifications obtainable in a modern TEM, when a suitably thinned foil is available, was a key element in this analysis.

Room Temperature Alkali Metal Reduction of Carbon Dioxide

2020 ◽  
Author(s):  
Lucas A. Freeman ◽  
Akachukwu D. Obi ◽  
Haleigh R. Machost ◽  
Andrew Molino ◽  
Asa W. Nichols ◽  
...  
Keyword(s):  
Alkali Metal ◽  
Alkali Metals ◽  
Room Temperature ◽  
Chemical Reduction ◽  
Bond Cleavage ◽  
Open Shell ◽  
Metal Reduction ◽  
One Pot ◽  
Earth Abundant ◽  
Electron Reduction

The reduction of the relatively inert carbon–oxygen bonds of CO<sub>2</sub> to access useful CO<sub>2</sub>-derived organic products is one of the most important fundamental challenges in synthetic chemistry. Facilitating this bond-cleavage using earth-abundant, non-toxic main group elements (MGEs) is especially arduous because of the difficulty in achieving strong inner-sphere interactions between CO<sub>2</sub> and the MGE. Herein we report the first successful chemical reduction of CO<sub>2</sub> at room temperature by alkali metals, promoted by a cyclic(alkyl)(amino) carbene (CAAC). One-electron reduction of CAAC-CO<sub>2</sub> adduct (<b>1</b>) with lithium, sodium or potassium metal yields stable monoanionic radicals clusters [M(CAAC–CO<sub>2</sub>)]<sub>n</sub>(M = Li, Na, K, <b> 2</b>-<b>4</b>) and two-electron alkali metal reduction affords open-shell, dianionic clusters of the general formula [M<sub>2</sub>(CAAC–CO<sub>2</sub>)]<sub>n </sub>(<b>5</b>-<b>8</b>). It is notable that these crystalline clusters of reduced CO<sub>2</sub> may also be isolated via the “one-pot” reaction of free CO<sub>2</sub> with free CAAC followed by the addition of alkali metals – a reductive process which does not occur in the absence of carbene. Each of the products <b>2</b>-<b>8</b> were investigated using a combination of experimental and theoretical methods.<br>

The Reactivity of Different Active Forms of Sodium Carbonate with Respect to Sulfur Dioxide

1992 ◽  
Vol 57 (11) ◽  
pp. 2302-2308
Author(s):  
Karel Mocek ◽  
Erich Lippert ◽  
Emerich Erdös
Keyword(s):  
Thermal Decomposition ◽  
Liquid Phase ◽  
Sulfur Dioxide ◽  
Specific Surface ◽  
Surface Area ◽  
Sodium Carbonate ◽  
Room Temperature ◽  
Active Form ◽  
The Other ◽  
Kinetics Of

The kinetics of the reaction of solid sodium carbonate with sulfur dioxide depends on the microstructure of the solid, which in turn is affected by the way and conditions of its preparation. The active form, analogous to that obtained by thermal decomposition of NaHCO3, emerges from the dehydration of Na2CO3 . 10 H2O in a vacuum or its weathering in air at room temperature. The two active forms are porous and have approximately the same specific surface area. Partial hydration of the active Na2CO3 in air at room temperature followed by thermal dehydration does not bring about a significant decrease in reactivity. On the other hand, if the preparation of anhydrous Na2CO3 involves, partly or completely, the liquid phase, the reactivity of the product is substantially lower.

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